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16153-59-6

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16153-59-6 Usage

General Description

(diethoxyphosphoryl)(phenyl)methyl acetate is a chemical compound with the molecular formula C12H17O5P. It is an ester derivative of phosphoric acid, containing two diethoxyphosphoryl groups, one phenyl group, one methyl group, and one acetate group. (diethoxyphosphoryl)(phenyl)methyl acetate is commonly used as a reagent in organic synthesis, particularly for the protection of hydroxyl groups in organic compounds. It can also act as a precursor for the synthesis of other phosphorus-containing compounds. Additionally, it has potential applications as an insecticide and as a chemical intermediate in the manufacturing of pharmaceuticals and agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 16153-59-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,5 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 16153-59:
(7*1)+(6*6)+(5*1)+(4*5)+(3*3)+(2*5)+(1*9)=96
96 % 10 = 6
So 16153-59-6 is a valid CAS Registry Number.

16153-59-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [diethoxyphosphoryl(phenyl)methyl] acetate

1.2 Other means of identification

Product number -
Other names 2-Acetoxy-benzylphosphonsaeure-diaethylester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:16153-59-6 SDS

16153-59-6Relevant articles and documents

A new, efficient, and simple method for the one-pot synthesis of α-acetoxyphosphonates from aldehydes under solvent-free conditions

Kaboudin, Babak,Karimi, Masoumeh

, p. 5324 - 5327 (2006)

A simple, efficient, and new method has been developed for the synthesis of α-acetoxyphosphonates from aldehydes through a one-pot reaction of aldehydes with diethylphosphite in the presence of acetic anhydride under solvent-free conditions using magnesiu

Iron-doped single-walled carbon nanotubes as new heterogeneous and highly efficient catalyst for acylation of alcohols, phenols, carboxylic acids and amines under solvent-free conditions

Sharghi, Hashem,Jokar, Mahboubeh,Doroodmand, Mohammad Mahdi

experimental part, p. 426 - 442 (2011/04/15)

Iron-doped single-walled carbon nanotubes (Fe/SWCNTs) represent an efficient and new heterogeneous reusable catalyst for the acylation of a variety of alcohols, phenols, carboxylic acids and amines with acid chlorides or acid anhydrides under solvent-free conditions. The reactions of various primary, secondary, tertiary, and benzylic alcohols, diols, phenols, as well as aromatic and aliphatic amines give acylated adducts in good to excellent yields.

Facile and high-yielding preparation of α-acetoxyphosphonates from α-hydroxyphosphonates assisted by microwave irradiation

Firouzabadi, Habib,Iranpoor, Nasser,Sobhani, Sara,Amoozgar, Zohreh

, p. 1771 - 1774 (2007/10/03)

A convenient and eco-friendly procedure is described for the efficient preparation of a variety of α-acetyloxyphosphonates from their corresponding α-hydroxyphosphonates using acetic anhydride under microwave irradiation in the absence of solvent.

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